Heba Baz
Cairo University
17 Papers
13 Citations
Heba Baz is an academic researcher from Cairo University. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 2, co-authored 12 publications.
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Papers
Establishment of reference intervals of clinical chemistry analytes for the adult population in Egypt.
Heba Baz,Kiyoshi Ichihara,May Selim,A. T. Awad,Sarah Aglan,Dalia Ibrahim Ramadan,Amina H Hassab,Lamia Mansour,Ola Elgaddar +8 more
TL;DR: In this article, the first Egyptian nationwide study for derivation of reference intervals (RIs) for 34 major chemistry analytes was conducted as a part of the global initiative by the IFCC Committee on Reference Intervals and Decision Limits (C-RIDL) for establishing country-specific RIs based on a harmonized protocol.
Genetic profiling of CAH Egyptian children: rapid guide to clinical interpretation of common mutations.
Fatma A. El-Mougy,Marwa Elsharkawy,Mona Hafez,Sahar Abdel Atty,Heba Baz,Amany Ibrahim,Hend Soliman,Sherif Ekladious,Mona Abdullatif,G. Thabet,Normeen Hany Rady,Alaa Afif,A. S. Tolba,Z. Zaki,Noha Musa +14 more
TL;DR: Strip hybridization assay is a rapid screening tool for the diagnosis of CAH and offers a rapid and easy guide for clinical reporting of common mutations for endocrinologists.
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Relation of serum vitamin D level in polycystic ovarian syndrome (PCOS) patients to ICSI outcome
Eman F. Omran,Abdelmaguid Ramzy,Amal Shohayeb,Nermeen Farouk,Mahmoud Soliman,Heba Baz,Marwa F. Sharaf +6 more
TL;DR: Serum vitamin D level is positively correlated with the number of retrieved and fertilized oocytes in PCOS patients undergoing ICSI cycles, and no significant correlation was found between the vitamin level and the occurrence of chemical or clinical pregnancy.
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CYP21A2 genetic profile in 14 Egyptian children with suspected congenital adrenal hyperplasia: a diagnostic challenge.
Fatma El-Mougy,Sahar A. Sharaf,Mona Hafez,Ahmed Khattab,Hazem Abou-Yousef,Marwa Elsharkawy,Heba Baz,Sherif Ekladious,Balsam Sherif,Noha Musa,Yasmin Elshiwy,Alaa Afif,Mona Abdullatif,Ghada Thabet,Normeen Hany Rady,Amany Ibrahim,Hend Soliman +16 more
TL;DR: This work reviews the diagnostic challenges despite an extensive genetic evaluation for 14 patients with a suspected clinical and biochemical diagnosis of congenital adrenal hyperplasia and suggests CYP21A2 mutations may help confirm the diagnosis.
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Allelic variants of insulin receptor substrate-1 gene in Egyptian women with polycystic ovary syndrome
TL;DR: The insulin receptor substrate gene-1 (IRS-1) polymorphisms have been incriminated in insulin resistance; a frequent finding in polycystic ovary syndrome (PCOS) and Screening for gly972arg genotype can be based on the HOMA quartile ranking.
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